Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K944348Substantially Equivalent

R&d Batteries, Inc. Part No. 5128, 5053, 5007

R & D Batteries, Inc., Burnsville MN / Traditional, Substantially Equivalent

K944348 is the FDA 510(k) clearance record for R&D BATTERIES, INC. PART NO. 5128, 5053, 5007, a class I device, cleared for R & D Batteries, Inc. on under FDA product code FCO (Box, Battery, Rechargeable). FDA records list 53 510(k) clearances for R & D Batteries, Inc., from to . As of , FDA records show no recalls naming K944348.

Clearance record

Decision date
Received
(198 days to decision)
Product code
FCO Box, Battery, Rechargeable
Regulation
21 CFR 876.1500
Device class
Class I
Review panel
Gastroenterology, Urology
Applicant
R & D Batteries, Inc. 2224 E. 117th St., Burnsville MN
510(k) summary
Statement
Third party review
No

Clearances, product code FCO

Trailing 12 months

FDA records hold no clearances under product code FCO in the trailing twelve months.

FDA records show no clearances under product code FCO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FCO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260